chr start stop reference nuc variant nuc depth genic status zygosity variant ID 3 129233411 129233412 G GGAAT 13 GENIC homozygous 693785939 3 129233449 129233450 A AATG 16 GENIC heterozygous 693785940 3 129237313 129237314 G A 22 GENIC homozygous 531262463 3 129243668 129243672 TCTG ---- 8 GENIC heterozygous 693785941 3 129247597 129247598 T - 14 GENIC homozygous 693785942 3 129248051 129248052 G GT 9 GENIC homozygous 693785943 3 129248202 129248203 T C 6 GENIC homozygous 528970899 3 129252065 129252066 C A 22 GENIC homozygous 531262464 3 129261603 129261604 C CT 21 GENIC homozygous 693785946 3 129262227 129262228 G - 17 GENIC homozygous 693785947 3 129265244 129265245 G C 16 GENIC homozygous 528970900 3 129265248 129265249 G T 16 GENIC possibly homozygous 528970901 3 129271336 129271337 T A 24 GENIC heterozygous 531262465 3 129271336 129271337 T TTGA 16 GENIC possibly homozygous 693785948 3 129274647 129274648 T G 6 GENIC homozygous 531262466 3 129274653 129274654 T G 6 GENIC homozygous 531262467 3 129278252 129278254 CA -- 14 GENIC heterozygous 693785951 3 129279324 129279325 G GA 6 GENIC heterozygous 693785952 3 129281582 129281583 A AG 19 GENIC homozygous 693785953 3 129281585 129281586 A - 16 GENIC homozygous 693785954 3 129285083 129285084 T - 12 GENIC heterozygous 693785955